HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(2-Bromopyridin-3-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-Bromo-3-(bromomethyl)pyridine | HCID 10901078 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Bromopyridin-3-yl)acetonitrile | HCID 53403509 | 83% |
Reaction Steps
A mixture of 2-bromo-3-bromomethyl-pyridine (840 mg, 3.35 mmol) and sodium cyanide (187.99 mg, 3.68 mmol) is stirred and refluxed for 1 h in a mixture water (10 mL)-ethanol (2 mL). The reaction mixture is diluted with dichloromethane and washed with saturated aqueous solution of sodium bicarbonate. The organic layer is separated, dried over magnesium sulfate and the solvent evaporated in vacuo to give 83% of the title compound that is used without further purification. MS (m/z): 197 (M+1), 199 (M+3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232289B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-259963ad65984f20a3e2916a844a5af0 |
| Source note | uspto-grants-2012_07 |